A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181298



Internal ID20748338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59139801..59154400hg38UCSC Ensembl
chr11:58907274..58921873hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3814600
hg1914600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472462
Supporting Variants
Samples
Known GenesFAM111A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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